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1. Full Text Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
by Eeles, Rosalind A and Olama, Ali Amin Al and Benlloch, Sara and Saunders, Edward J and Leongamornlert, Daniel A and Tymrakiewicz, Malgorzata and Ghoussaini, Maya and Luccarini, Craig and Dennis, Joe and Jugurnauth-Little, Sarah and Dadaev, Tokhir and Neal, David E and Hamdy, Freddie C and Donovan, Jenny L and Muir, Ken and Giles, Graham G and Severi, Gianluca and Wiklund, Fredrik and Gronberg, Henrik and Haiman, Christopher A and Schumacher, Fredrick and Henderson, Brian E and Le Marchand, Loic and Lindstrom, Sara and Kraft, Peter and Hunter, David J and Gapstur, Susan and Chanock, Stephen J and Berndt, Sonja I and Albanes, Demetrius and Andriole, Gerald and Schleutker, Johanna and Weischer, Maren and Canzian, Federico and Riboli, Elio and Key, Tim J and Travis, Ruth C and Campa, Daniele and Ingles, Sue A and John, Esther M and Hayes, Richard B and Pharoah, Paul D. P and Pashayan, Nora and Khaw, Kay-Tee and Stanford, Janet L and Ostrander, Elaine A and Signorello, Lisa B and Thibodeau, Stephen N and Schaid, Dan and Maier, Christiane and Vogel, Walther and Kibel, Adam S and Cybulski, Cezary and Lubinski, Jan and Cannon-Albright, Lisa and Brenner, Hermann and Park, Jong Y and Kaneva, Radka and Batra, Jyotsna and Spurdle, Amanda B and Clements, Judith A and Teixeira, Manuel R and Dicks, Ed and Lee, Andrew and Dunning, Alison M and Baynes, Caroline and Conroy, Don and Maranian, Melanie J and Ahmed, Shahana and Govindasami, Koveela and Guy, Michelle and Wilkinson, Rosemary A and Sawyer, Emma J and Morgan, Angela and Dearnaley, David P and Horwich, Alan and Huddart, Robert A and Khoo, Vincent S and Parker, Christopher C and Van As, Nicholas J and Woodhouse, Christopher J and Thompson, Alan and Dudderidge, Tim and Ogden, Chris and Cooper, Colin S and Lophatananon, Artitaya and Cox, Angela and Southey, Melissa C and Hopper, John L and English, Dallas R and Aly, Markus and Adolfsson, Jan and Xu, Jiangfeng and Zheng, Siqun L and Yeager, Meredith and Kaaks, Rudolf and Diver, W Ryan and Gaudet, Mia M and Stern, Mariana C and Corral, Roman and ... and UK Genetic Prostate Canc Study and Australian Prostate Canc and PRACTICAL Prostate Canc Assoc Grp and COGS-Canc Res UK GWAS-ELLIPSE Part and UK ProtecT Prostate Testing Canc and COGS–Cancer Research UK GWAS–ELLIPSE (part of GAME-ON) Initiative and UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons' Section of Oncology and UK ProtecT (Prostate testing for cancer and Treatment) Study Collaborators and Australian Prostate Cancer Bioresource and PRACTICAL (Prostate Cancer Association Group to Investigate Cancer-Associated Alterations in the Genome) Consortium and The PRACTICAL (Prostate Cancer Association Group to Investigate Cancer-Associated Alterations in the Genome) Consortium and The Australian Prostate Cancer Bioresource and The UK ProtecT (Prostate testing for cancer and Treatment) Study Collaborators and The COGS–Cancer Research UK GWAS–ELLIPSE (part of GAME-ON) Initiative and The UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons' Section of Oncology
Nature Genetics, ISSN 1061-4036, 04/2013, Volume 45, Issue 4, pp. 385 - 391
Prostate cancer is the most frequently diagnosed cancer in males in developed countries. To identify common prostate cancer susceptibility alleles, we... 
VARIANTS | PREDISPOSITION | MEN | GENETICS & HEREDITY | MUTATIONS | HOXB13 | GENOME-WIDE ASSOCIATION | Prostatic Neoplasms - pathology | Genetic Predisposition to Disease | Genome-Wide Association Study | Meta-Analysis as Topic | Oligonucleotide Array Sequence Analysis | Humans | Risk Factors | Genetic Loci - genetics | Prostatic Neoplasms - etiology | Cooperative Behavior | Genotype | Male | Case-Control Studies | Polymorphism, Single Nucleotide - genetics | Quantitative trait loci | Genetic susceptibility | Genetic aspects | Research | Prostate cancer | Identification and classification | Risk factors | Studies | Confidence intervals | Genotype & phenotype | Genealogy | Quality control | Cell cycle | Genomes | DNA repair | Deoxyribonucleic acid--DNA | Klinisk medicin | Medicin och hälsovetenskap | Cancer och onkologi
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2. Full Text The oncoarray consortium: A network for understanding the genetic architecture of common cancers
by Amos, Christopher I and Dennis, Joe and Wang, Zhaoming and Byun, Jinyoung and Schumacher, Fredrick R and Gayther, Simon A and Casey, Graham and Hunter, David J and Sellers, Thomas A and Gruber, Stephen B and Dunning, Alison M and Michailidou, Kyriaki and Fachal, Laura and Doheny, Kimberly and Spurdle, Amanda B and Li, Yafang and Xiao, Xiangjun and Romm, Jane and Pugh, Elizabeth and Coetzee, Gerhard A and Hazelett, Dennis J and Bojesen, Stig E and Caga-Anan, Charlisse and Haiman, Christopher A and Kamal, Ahsan and Luccarini, Craig and Tessier, Daniel and Vincent, Daniel and Bacot, Francois and Van Den Berg, David J and Nelson, Stefanie and Demetriades, Stephen and Goldgar, David E and Couch, Fergus J and Forman, Judith L and Giles, Graham G and Conti, David V and Bickeboller, Heike and Risch, Angela and Waldenberger, Melanie and Bruske-Hohlfeld, Irene and Hicks, Belynda D and Ling, Hua and McGuffog, Lesley and Lee, Andrew and Kuchenbaecker, Karoline and Soucy, Penny and Manz, Judith and Cunningham, Julie M and Butterbach, Katja and Kote-Jarai, Zsofia and Kraft, Peter and FitzGerald, Liesel and Lindstrom, Sara and Adams, Marcia and McKay, James D and Phelan, Catherine M and Benlloch, Sara and Kelemen, Linda E and Brennan, Paul and Riggan, Marjorie and O'Mara, Tracy A and Shen, Hongbing and Shi, Yongyong and Thompson, Deborah J and Goodman, Marc T and Nielsen, Sune F and Berchuck, Andrew and Laboissiere, Sylvie and Schmit, Stephanie L and Shelford, Tameka and Edlund, Christopher K and Taylor, Jack A and Field, John K and Park, Sue K and Offit, Kenneth and Thomassen, Mads and Schmutzler, Rita and Ottini, Laura and Hung, Rayjean J and Marchini, Jonathan and Olama, Ali Amin Al and Peters, Ulrike and Eeles, Rosalind A and Seldin, Michael F and Gillanders, Elizabeth and Seminara, Daniela and Antoniou, Antonis C and Pharoah, Paul D.P and Chenevix-Trench, Georgia and Chanock, Stephen J and Simard, Jacques and Easton, Douglas F
Cancer Epidemiology Biomarkers and Prevention, ISSN 1055-9965, 01/2017, Volume 26, Issue 1, pp. 126 - 135
Background: Common cancers develop through a multistep process often including inherited susceptibility. Collaboration among multiple institutions, and funding... 
BREAST-CANCER | LUNG | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | VARIANTS | RARE | ONCOLOGY | ENVIRONMENT INTERACTIONS | PROSTATE-CANCER | SUSCEPTIBILITY LOCI | RISK | MENDELIAN RANDOMIZATION | GENOME-WIDE ASSOCIATION | Causation | Health risks | Principal components analysis | Genomes | Pharmacology | Mapping | Single-nucleotide polymorphism | Environmental impact | Loci | Ethnic factors | Impact analysis | Ecological risk assessment | Consortia | Genetic variance | Genotyping | Etiology | Risk assessment | Quality control | Tagging | Biomarkers | Gene mapping | Cancer | Ancestry | Epistasis | Genetic Susceptibility | Genetic Epidemiology
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3. Full Text Impact of the G84E variant on HOXB13 gene and protein expression in formalin-fixed, paraffin-embedded prostate tumours
by Fitzgerald, Liesel M and Raspin, Kelsie and Marthick, James R and Field, Matt A and Malley, Roslyn C and Thomson, Russell J and Blackburn, Nicholas B and Banks, Annette and Charlesworth, Jac C and Donovan, Shaun and Dickinson, Joanne L
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 17778 - 9
The HOXB13 G84E variant is associated with risk of prostate cancer (PCa), however the role this variant plays in PCa development is unknown. This study... 
Genetic Predisposition to Disease - genetics | Gene Expression - genetics | Humans | Risk Factors | Tasmania | Formaldehyde - pharmacology | Genotype | Male | DNA Methylation - genetics | Case-Control Studies | Homeodomain Proteins - genetics | Paraffin Embedding - methods | Prostatic Neoplasms - genetics | Alleles | Heterozygote | Genetic Variation - genetics | Transcription, Genetic - genetics | Cohort Studies | Immunohistochemistry | Proteins | Transcription | DNA methylation | Protein expression | Paraffin | Prostate | Prostate cancer | CpG islands | Tumors | Hoxb13 gene
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4. Full Text Discovery of common and rare genetic risk variants for colorectal cancer
by Huyghe, Jeroen R and Bien, Stephanie A and Harrison, Tabitha A and Kang, Hyun Min and Chen, Sai and Schmit, Stephanie L and Conti, David V and Qu, Conghui and Jeon, Jihyoun and Edlund, Christopher K and Greenside, Peyton and Wainberg, Michael and Schumacher, Freick R and Smith, Joshua D and Levine, David M and Nelson, Sarah C and Sinnott-Armstrong, Nasa A and Albanes, Demetrius and Alonso, M. Henar and Anderson, Kristin and Arnau-Collell, Coral and Arndt, Volker and Bamia, Christina and Banbury, Barbara L and Baron, John A and Berndt, Sonja I and Bézieau, Stéphane and Bishop, D. Timothy and Boehm, Juergen and Boeing, Heiner and Brenner, Hermann and Brezina, Stefanie and Buch, Stephan and Buchanan, Daniel D and Burnett-Hartman, Anea and Butterbach, Katja and Caan, Bette J and Campbell, Peter T and Carlson, Christopher S and Castellví-Bel, Sergi and Chan, Anew T and Chang-Claude, Jenny and Chanock, Stephen J and Chirlaque, Maria Dolores and Cho, Sang Hee and Connolly, Charles M and Cross, Amanda J and Cuk, Katarina and Curtis, Keith R and de la Chapelle, Albert and Doheny, Kimberly F and Duggan, David and Easton, Douglas F and Elias, Sjoerd G and Elliott, Faye and English, Dallas R and Feskens, Edith J.M and Figueiredo, Jane C and Fischer, Rocky and FitzGerald, Liesel M and Forman, David and Gala, Manish and Gallinger, Steven and Gauderman, W. James and Giles, Graham G and Gillanders, Elizabeth and Gong, Jian and Goodman, Phyllis J and Grady, William M and Grove, John S and Gsur, Anea and Gunter, Marc J and Haile, Robert W and Hampe, Jochen and Hampel, Heather and Harlid, Sophia and Hayes, Richard B and Hofer, Philipp and Hoffmeister, Michael and Hopper, John L and Hsu, Wan Ling and Huang, Wen Yi and Hudson, Thomas J and Hunter, David J and Ibañez-Sanz, Gemma and Idos, Gregory E and Ingersoll, Roxann and Jackson, Rebecca D and Jacobs, Eric J and Jenkins, Mark A and Joshi, Amit D and Joshu, Corinne E and Keku, Temitope O and Key, Timothy J and Kim, Hyeong Rok and Kobayashi, Emiko and Kolonel, Laurence N and Kooperberg, Charles and Kühn, Tilman and Küry, Sébastien and ... and Medicinska fakulteten and Institutionen för strålningsvetenskaper and Onkologi and Umeå universitet
Nature Genetics, ISSN 1061-4036, 01/2019, Volume 51, Issue 1, pp. 76 - 87
To further dissect the genetic architecture of colorectal cancer (CRC), we performed whole-genome sequencing of 1,439 cases and 720 controls, imputed... 
Genetics | Journal Article | COLON-CANCER | ORGAN SIZE | METAANALYSIS | LYSOPHOSPHATIDIC ACID | GENETICS & HEREDITY | SUSCEPTIBILITY LOCI | QUALITY-CONTROL | MUTATIONS | EXPRESSION | GENOME-WIDE ASSOCIATION | IDENTIFIES 6 | Genetic Predisposition to Disease - genetics | Colorectal Neoplasms - genetics | Humans | Middle Aged | Risk Factors | Genotype | Male | RNA, Long Noncoding - genetics | Signal Transduction - genetics | Case-Control Studies | Polymorphism, Single Nucleotide - genetics | Female | Aged | Genome-Wide Association Study - methods | Genetic aspects | Research | Genetic variation | Risk factors | Colorectal cancer | Haplotypes | Immune response | Nucleotide sequence | Colorectal carcinoma | Health risks | Risk | Systematic review | Genomes | Drug development | Gene expression | Epidemiology | Gene sequencing | Meta-analysis | Consortia | Yes-associated protein | Studies | Signaling | Hedgehog protein | Gastroenterology | Heritability | Mutation | Cancer | Life Sciences | Santé publique et épidémiologie | Basic Medicine | Medical Genetics | Medicinsk genetik | Clinical Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Cancer and Oncology | Klinisk medicin | Cancer och onkologi
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5. Full Text Association of TMPRSS2-ERG gene fusion with clinical characteristics and outcomes: Results from a population-based study of prostate cancer
by FitzGerald, Liesel M and Agalliu, Ilir and Johnson, Karynn and Miller, Melinda A and Kwon, Erika M and Hurtado-Coll, Antonio and Fazli, Ladan and Rajput, Ashish B and Gleave, Martin E and Cox, Michael E and Ostrander, Elaine A and Stanford, Janet L and Huntsman, David G
BMC Cancer, ISSN 1471-2407, 08/2008, Volume 8, Issue 1, pp. 230 - 230
Background: The presence of the TMPRSS2-ERG fusion gene in prostate tumors has recently been associated with an aggressive phenotype, as well as recurrence and... 
HETEROGENEITY | OVEREXPRESSION | TRANSCRIPTS | ONCOLOGY | FREQUENCY | IN-SITU HYBRIDIZATION | FISH | RISK | REARRANGEMENTS | EXPRESSION | Prostatic Neoplasms - metabolism | Prostatic Neoplasms - pathology | Humans | Middle Aged | Genotype | In Situ Hybridization, Fluorescence | Male | Treatment Outcome | Oncogene Proteins, Fusion - physiology | Microarray Analysis | Oncogene Fusion | Oncogene Proteins, Fusion - genetics | Aged, 80 and over | Adult | Prostatectomy | Aged | Polymorphism, Single Nucleotide | Physiological aspects | Genetic aspects | Research | Diagnosis | Prostate cancer | Gene fusion
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6. Full Text Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
by Eeles, R.A and Kote Jarai, Z and Al Olama, A.A and Giles, G.G and Guy, M and Severi, G and Muir, K and Hopper, J.L and Henderson, B.E and Haiman, C.A and Schleutker, J and Hamdy, F.C and Neal, D.E and Donovan, J.L and Stanford, J.L and Ostrander, E.A and Ingles, S.A and John, E.M and Thibodeau, S.N and Schaid, D and Park, J.Y and Spurdle, A and Clements, J and Dickinson, J.L and Maier, C and Vogel, W and Dork, T and Rebbeck, T.R and Cooney, K.A and Cannon Albright, L and Chappuis, P.O and Hutter, P and Zeegers, M and Kaneva, R and Zhang, H.W and Lu, Y.J and Foulkes, WD and English, D.R and Leongamornlert, D.A and Tymrakiewicz, M and Morrison, J and Ardern Jones, A.T and Hall, A.L and O'Brien, L.T and Wilkinson, R.A and Saunders, E.J and Page, E.C and Sawyer, E.J and Edwards, S.M and Dearnaley, D.P and Horwich, A and Huddart, R.A and Khoo, V.S and Parker, C.C and Van As, N and Woodhouse, C.J and Thompson, A and Christmas, T and Ogden, C and Cooper, C.S and Southey, M.C and Lophatananon, A and Liu, J.F and Kolonel, L.N and Le Marchand, L and Wahlfors, T and Tammela, T.L and Auvinen, A and Lewis, S.J and Cox, A and FitzGerald, L.M and Koopmeiners, J.S and Karyadi, D.M and Kwon, E.M and Stern, M.C and Corral, R and Joshi, A.D and Shahabi, A and McDonnell, S.K and Sellers, T.A and Pow Sang, J and Chambers, S and Aitken, J and Gardiner, R.A and Batra, J and Kedda, M.A and Lose, F and Polanowski, A and Patterson, B and Serth, J and Meyer, A and Luedeke, M and Stefflova, K and Ray, A.M and Lange, E.M and Farnham, J and Khan, H and Slavov, C and Mitkova, A and British Assoc Urological Surg and PRACTICAL Consortium and UK ProtecT Study Collaborators and UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons' Section of Oncology and The PRACTICAL Consortium and The UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons' Section of Oncology and The UK ProtecT Study Collaborators
Nature Genetics, ISSN 1061-4036, 01/2009, Volume 41, Issue 10, pp. 1116 - 21
Prostate cancer (PrCa) is the most frequently diagnosed cancer in males in developed countries. To identify common PrCa susceptibility alleles, we previously... 
RISK | AUSTRALIAN CASE-CONTROL | VARIANTS | MULTIPLE | GENETICS & HEREDITY | ANTIGEN | Genome-Wide Association Study | Disease Susceptibility | Prostatic Neoplasms - genetics | Humans | Genotype | Male | Chromosomes, Human | Polymorphism, Single Nucleotide | Genome, Human | Disease susceptibility | Genetic aspects | Research | Diagnosis | Single nucleotide polymorphisms | Health aspects | Prostate cancer | Risk factors | Studies | Medical research | Inflation | Regression analysis | Chromosomes
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7. Full Text Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
by Schumacher, Fredrick R and Al Olama, Ali Amin and Berndt, Sonja I and Benlloch, Sara and Ahmed, Mahbubl and Saunders, Edward J and Dadaev, Tokhir and Leongamornlert, Daniel and Anokian, Ezequiel and Cieza-Borrella, Clara and Goh, Chee and Brook, Mark N and Sheng, Xin and Fachal, Laura and Dennis, Joe and Tyrer, Jonathan and Muir, Kenneth and Lophatananon, Artitaya and Stevens, Victoria L and Gapstur, Susan M and Carter, Brian D and Tangen, Catherine M and Goodman, Phyllis J and Thompson, Ian M and Batra, Jyotsna and Chambers, Suzanne and Moya, Leire and Clements, Judith and Horvath, Lisa and Tilley, Wayne and Risbridger, Gail P and Gronberg, Henrik and Aly, Markus and Nordström, Tobias and Pharoah, Paul and Pashayan, Nora and Schleutker, Johanna and Tammela, Teuvo L. J and Sipeky, Csilla and Auvinen, Anssi and Albanes, Demetrius and Weinstein, Stephanie and Wolk, Alicja and Håkansson, Niclas and West, Catharine M. L and Dunning, Alison M and Burnet, Neil and Mucci, Lorelei A and Giovannucci, Edward and Andriole, Gerald L and Cussenot, Olivier and Cancel-Tassin, Géraldine and Koutros, Stella and Beane Freeman, Laura E and Sorensen, Karina Dalsgaard and Orntoft, Torben Falck and Borre, Michael and Maehle, Lovise and Grindedal, Eli Marie and Neal, David E and Donovan, Jenny L and Hamdy, Freddie C and Martin, Richard M and Travis, Ruth C and Key, Tim J and Hamilton, Robert J and Fleshner, Neil E and Finelli, Antonio and Ingles, Sue Ann and Stern, Mariana C and Rosenstein, Barry S and Kerns, Sarah L and Ostrer, Harry and Lu, Yong-Jie and Zhang, Hong-Wei and Feng, Ninghan and Mao, Xueying and Guo, Xin and Wang, Guomin and Sun, Zan and Giles, Graham G and Southey, Melissa C and MacInnis, Robert J and Fitzgerald, Liesel M and Kibel, Adam S and Drake, Bettina F and Vega, Ana and Gómez-Caamaño, Antonio and Szulkin, Robert and Eklund, Martin and Kogevinas, Manolis and Llorca, Javier and Castaño-Vinyals, Gemma and Penney, Kathryn L and Stampfer, Meir and Park, Jong Y and Sellers, Thomas A and Lin, Hui-Yi and Stanford, Janet L and Cybulski, Cezary and ... and Profile Study and Canary PASS Investigators and Canc Prostate Sweden CAPS and IMPACT Study and Prostate Canc Genome-wide As and APCB and Breast Prostate Canc Cohort Consor and PRACTICAL Prostate Canc As and Genetic Assoc Mech Oncology GAME and Breast and Prostate Cancer Cohort Consortium (BPC3) and Prostate Cancer Genome-wide Association Study of Uncommon Susceptibility Loci (PEGASUS) and Australian Prostate Cancer BioResource (APCB) and Genetic Associations and Mechanisms in Oncology (GAME-ON)/Elucidating Loci Involved in Prostate Cancer Susceptibility (ELLIPSE) Consortium and Cancer of the Prostate in Sweden (CAPS) and PRACTICAL (Prostate Cancer Association Group to Investigate Cancer-Associated Alterations in the Genome) Consortium and The PRACTICAL (Prostate Cancer Association Group to Investigate Cancer-Associated Alterations in the Genome) Consortium and The IMPACT Study and The Profile Study and The Genetic Associations and Mechanisms in Oncology (GAME-ON)/Elucidating Loci Involved in Prostate Cancer Susceptibility (ELLIPSE) Consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Ortopedi and Uppsala universitet and Institutionen för kirurgiska vetenskaper
Nature Genetics, ISSN 1061-4036, 07/2018, Volume 50, Issue 7, pp. 928 - 936
Genome-wide association studies (GWAS) and fine-mapping efforts to date have identified more than 100 prostate cancer (PrCa)-susceptibility loci. We... 
CONSORTIUM | METAANALYSIS | GENE | VARIANTS | PATHWAY | GENETICS & HEREDITY | RISK | MULTIPLE LOCI | IDENTIFICATION | GENOME-WIDE ASSOCIATION | PREDICTION | Genetic Predisposition to Disease | Prostatic Neoplasms - genetics | Humans | Genotype | Male | Risk | Polymorphism, Single Nucleotide | Genetic Loci | Genome-Wide Association Study - methods | Case-Control Studies | Case studies | Genome-wide association studies | Usage | Men | Genetic aspects | Health aspects | Prostate cancer | Risk factors | Genealogy | Data processing | Genomes | Mapping | Biology | Family medical history | Loci | Meta-analysis | Confidence intervals | Consortia | Signal transduction | Software | Gene mapping | Health risk assessment | Prostate | Genotypes | Cancer | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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